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Legal - Product Liability
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EXPERT VIEW
In praise of the CE marking, but medtech's worst fear is still alive
06 July 2010
Ashley Yeo
The European Medicines Agency review meeting in London on 30 June passed with scarcely a mention of devices and diagnostics. This was perhaps as expected, given that the meeting, held to examine the outcomes of the assessment of Ernst & Young's ...
LATEST FEATURES
How Manufacturers Can Ensure Control over Subcontractors in the EU
16 November 2009
Erik Vollebregt explains how medical device manufacturers entering into agreements with subcontractors can safeguard their rights and avoid exposure ...
New French Case Law on Product Liability: Changes and Controversies
21 September 2009
Cécile Derycke and Agnès Roman-Amat discuss the implications of a Civil Supreme Court decision on “defects” and “causal relationships”. The French ...
The US Medical Device Safety Act - Legislation Too Far
20 July 2009
When the US Congress enacted the Medical Devices Amendments to the Federal Food, Drug, and Cosmetic Act in 1976, it recognised that medical devices ...
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LATEST COUNTRY PROFILES
Trademarks Briefing (Devices) - Luxembourg
08 October 2009
Please give details of the major acts and directives governing trademarks. Trademarks are governed in Luxembourg by the: Benelux Convention on ...
Regulation of Medical Devices Briefing - Spain
08 October 2009
1) Which authority is responsible for overseeing the regulation of medical devices and diagnostics in Spain? Agencia Española del Medicamento, the ...
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MULTIMEDIA
RAJ Devices News Roundup, July 2010
19 July 2010
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